ODCs

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1 OMIM reference -
4 associated genes
No signs/symptoms info

COMMON GENES: 1
PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Dejerine-Sottas syndrome

Autosomal dominant Charcot-Marie-Tooth disease type 2I


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PMP22	(0.94)	MPZ

Citations in the biomedical literature:

Dejerine-Sottas syndrome		Autosomal dominant Charcot-Marie-Tooth disease type 2I
	Synonym(s): - Charcot-Marie-Tooth disease type 3 - HMSN 3 - Hereditary motor and sensory neuropathy type 3 - Hypertrophic neuropathy of infancy		Synonym(s): - CMT2I

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C538392		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.